Reactome: A Curated Pathway Database
THIS SITE IS USED FOR CURATION AND TESTING
IT IS NOT STABLE, IS LINKED TO AN INCOMPLETE DATA SET, AND IS NOT MONITORED FOR PERFORMANCE. WE STRONGLY RECOMMEND THE USE OF OUR PUBLIC SITE

Query author contributions in Reactome

Reactome depends on collaboration between our curation team and outside experts to assemble and peer-review its pathway modules. The integration of ORCID within Reactome enables us to meet a key challenge with authoring, curating and reviewing biological information by incentivizing and crediting the external experts that contribute their expertise and time to the Reactome curation process. More information is available at ORCID and Reactome.

If you have an ORCID ID that is not listed on this page, please forward this information to us and we will update your Reactome pathway records.

Name Email address

Details on Person Tuddenham, E G

Class:IdPerson:9661582
_displayNameTuddenham, E G
_timestamp2019-09-18 08:33:15
created[InstanceEdit:9661631] Shamovsky, Veronica, 2019-09-18
firstnameE G
initialEG
surnameTuddenham
(author)[LiteratureReference:9661601] Distribution of factor VIII mRNA and antigen in human liver and other tissues
[LiteratureReference:9661667] Expression of active human factor VIII from recombinant DNA clones
[LiteratureReference:9661977] Stable recombinant expression and characterization of the two haemophilic factor VIII variants C329S (CRM(-)) and G1948D (CRM(r))
[LiteratureReference:9662705] Molecular etiology of factor VIII deficiency in hemophilia A
[LiteratureReference:9666401] Purification and characterization of factor VIII 1,689-Cys: a nonfunctional cofactor occurring in a patient with severe hemophilia A
[LiteratureReference:9667108] CRM+ haemophilia A due to a missense mutation (372----Cys) at the internal heavy chain thrombin cleavage site
[LiteratureReference:9667111] Purification and characterization of factor VIII 372-Cys: a hypofunctional cofactor from a patient with moderately severe hemophilia A
[LiteratureReference:9667112] Factor VIII S373L: mutation at P1' site confers thrombin cleavage resistance, causing mild haemophilia A
[LiteratureReference:9670003] A molecular model for the triplicated A domains of human factor VIII based on the crystal structure of human ceruloplasmin
[LiteratureReference:9671812] An interactive mutation database for human coagulation factor IX provides novel insights into the phenotypes and genetics of hemophilia B
[Change default viewing format]
No pathways have been reviewed or authored by Tuddenham, E G (9661582)